Inhibition of monkey brain semicarbazide-sensitive amine oxidase by various antidepressants

被引:11
作者
Obata, T [1 ]
Yamanaka, Y [1 ]
机构
[1] Oita Med Univ, Dept Pharmacol, Hasama, Oita 8795593, Japan
关键词
antidepressant; semicarbazide-sensitive amine oxidase; semicarbazide; benzylamine; monkey brain;
D O I
10.1016/S0304-3940(00)01087-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We examined whether the antidepressant drugs, such as the dicyclic drug zimeldine, the tricyclic drug imipramine, tetracyclic drug maprotiline, and the non-cyclic drug nomifensine, inhibit in vitro semicarbazide-sensitive amine oxidase (SSAO) activity in monkey brain. The deamination of 1 mu M benzylamine was not inhibited at high concentrations of clorgyline or deprenyl, while it was highly sensitive for semicarbazide, When corresponding experiments were performed with 100 mu M benzylamine, the opposite results were obtained. The most potent of inhibition of SSAO was observed by imipramine, followed by maprotiline, zimeldine and nomifensine. Inhibition of SSAO was not enhanced by varying the time of preincubation of the enzyme and various antidepressant drugs, indicating direct action on and reversible inhibition of SSAO. We found the tricyclic antidepressant drug to be the most selective inhibitors of SSAO activity in monkey brain, as compared with other type of antidepressant drugs. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:131 / 133
页数:3
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